Responsibilities

- Supports the execution of regulatory planning and operational activities across LATAM for Electrophysiology (EP) and Neurovascular (NV) portfolios
- Supports dossier delivery to Local Operating Companies (LoCs)
- Contributes to data-driven decision-making and drives process standardization to enable efficient lifecycle management (LCM) and new product introductions (NPI)
- Executes the preparation and delivery of regulatory dossiers to LoCs ensuring completeness and compliance with local requirements
- Tracks dossier submission timelines and ensures alignment with regulatory action plans and market needs
- Supports document management activities, including version control
- Acts as a liaison between regional teams and LoCs to ensure clarity on dossier requirements
- Contributes to planning and forecasting activities




- Maintains regional trackers, dashboards, and planning tools
- Consolidates and analyzes regulatory performance metrics
- Identifies opportunities to improve planning, dossier delivery, and operational processes

Requirements

- Bachelor’s degree in Pharmacy, Engineering, Life Sciences, or related field
- 0–2 years of experience in Regulatory Affairs or related field
- Strong analytical and problem‑solving skills
- High attention to detail and process orientation
- Proficiency in Excel; data visualization tools (e.g., Power BI) is a plus
- Advanced or intermediate skills in English/ Spanish is preferred.

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📌 Regulatory Affairs Analyst (Lima)
🏢 Jobtailor
📍 Lima